4.4 Article

Baseline serum TSH levels predict the absence of thyroid dysfunction in cancer patients treated with immunotherapy

Journal

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
Volume 44, Issue 8, Pages 1719-1726

Publisher

SPRINGER
DOI: 10.1007/s40618-020-01480-6

Keywords

Immunotherapy; Thyroid dysfunction; TSH; Anti-thyroid antibodies; PD-1; PD-L1

Funding

  1. Universita degli Studi di Siena within the CRUI-CARE Agreement

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This study aimed to identify predictive factors for the development of thyroid dysfunction during immunotherapy in patients with metastatic or unresectable advanced cancers treated with immune checkpoint inhibitors. Results showed that pre-treatment serum TSH and ATAbs levels may help to identify patients at high risk for primary thyroid dysfunction. This suggests guidance for appropriate screening and management of thyroid dysfunctions in patients undergoing ICIs treatment.
Purpose Immunotherapy against immune checkpoints has significantly improved survival both in metastatic and adjuvant setting in several types of cancers. Thyroid dysfunction is the most common endocrine adverse event reported. Patients who are at risk of developing thyroid dysfunction remain to be defined. We aimed to identify predictive factors for the development of thyroid dysfunction during immunotherapy. Methods This is a retrospective study including a total of 68 patients who were treated with immune checkpoint inhibitors (ICIs) for metastatic or unresectable advanced cancers. The majority of patients were treated with anti-PD1 drugs in monotherapy or in combination with anti-CTLA4 inhibitors. Thyroid function and anti-thyroid antibodies, before starting immunotherapy and during treatment, were evaluated. Thyroid ultrasound was also performed in a subgroup of patients at the time of enrolment in the study. Results Eleven out of 68 patients (16.1%) developed immune-related overt thyroid dysfunction. By ROC curve analysis, we found that a serum TSH cut-off of 1.72 mUI/l, at baseline, had a good diagnostic accuracy in identifying patients without overt thyroid dysfunction (NPV = 100%, p = 0.0029). At multivariate analysis, both TSH and positive anti-thyroid antibodies (ATAbs) levels, before ICIs treatment, were independently associated with the development of overt thyroid dysfunction during immunotherapy (p = 0.0001 and p = 0.009, respectively). Conclusions Pre-treatment serum TSH and ATAbs levels may help to identify patients at high risk for primary thyroid dysfunction. Our study suggests guidance for an appropriate timely screening and for a tailored management of thyroid dysfunctions in patients treated with ICIs.

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